Tag | Content |
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EnhancerAtlas ID | HS063-02075 |
Organism | Homo sapiens |
Tissue/cell | GM18505 |
Coordinate | chr16:9146430-9147460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr16:9146646-9146661 | TGAACTTCTGACCTC | - | 6.38 | RARA | MA0729.1 | chr16:9146643-9146661 | TCTTGAACTTCTGACCTC | - | 6.88 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I009052 | chr16 | 9146584 | 9147670 |
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Enhancer Sequence | ACGAAGCTCA GATTTTTTTG ATTTTTTTTT TTTTTTTTTT TCTGCCCAGG CTGGAGTGCA 60 ATGGCGCTAT CTCATTGCAA CCTCTACCTC CCAGGTTCAA GCCATTCTCC TGCATCAGCC 120 TCCCAAGGAG CTGGGATTAC AGGCGTCCAC CACCACACCT GGCTAATCTG TATTTTTAGT 180 AGGGATGGCG TTTCCCCATG TTGGTCAGGC TGGTCTTGAA CTTCTGACCT CAGGTTATCC 240 GCCTGCCTCG GCCTCCCAAA GCGCTGGGAT TAGAGGCGTG TGCTCCCGCG CCCGGCCCTG 300 AGCTCAACTT TTTAAGGTGG ATTTGATATA ACGGCTGTGT ATTACTTAAG AGAACACGAG 360 CCACCGTAAC AAAGAAACCC TCAAAAGGAC AAAAAAAACA AAAACAAAAA CAAAAAACCC 420 GAAAATAAAC CCCCAAATCT CAGTGGCCTA ACACAAGGAG AATTTATTTC TTGCTCATAT 480 AAAGTCCAAA ACTGGTATTC CTGATAGGCA GGTGGCTCTC TTCCATTACC TGATCCAGGG 540 ACCCACGCTC CTGCTTGCTC GGGGCTCTGC TTTCTCCATC AGGATGAGTA AAATGCAGGA 600 GCACGGAGGT CAGCCCAGGA GGTGGTTACT AGCAAGGCCA CTAGCACGGG GTTGGGGGAA 660 TGCCTCTCCT TGCATTCCTT TGGCCCAAAT CCAGTCACGT GCCCACCCTC AACAGCAAGG 720 GATGCTGGGA AATGTAGTCC AGCCACAAGC CAAGGAGGTG GCCAGGAACA GCCTTTGGCC 780 AACTCGGAGG CCCTGAGTGA TCTGAGTCTG AGCTCACACC ACCTTCCTCA TTCACTACGC 840 TGTAGGTACA TTGATTCCTA TAGTTCCCCC AAATGAAAAC CTCTTTCCTA CCTCAGCTTT 900 TGCCCGGGCT ATTCCTTCTG CCTAAAATGC CCTCCTCCTC TGTCCACCTG GCTGGTTCCT 960 TGCCATCCTT CAGGTCTCAG CATGGGGATC CTCTTCTGAG AAGCCTCTTA TGACCGTGCC 1020 ATCAAAAAAA 1030
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